Canonical Allele Identifier: CA363279688
Gene: DCDC2 HGNC NCBI

Linked Data

gnomAD v4: 6-24178353-C-G
MyVariant Identifiers: chr6:g.24178581C>G (hg19) chr6:g.24178353C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178353C>G , CM000668.2:g.24178353C>G GRCh38
NC_000006.11:g.24178581C>G , CM000668.1:g.24178581C>G GRCh37
NC_000006.10:g.24286560C>G NCBI36
NG_012829.1:g.184700G>C
NG_012829.2:g.209940G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1303G>C MANE Select ENSP00000367715.3:p.Gly435Arg
ENST00000378450.6:c.562G>C ENSP00000367711.3:p.Gly188Arg
ENST00000378454.7:c.1303G>C ENSP00000367715.3:p.Gly435Arg
NM_001195610.1:c.1303G>C NP_001182539.1:p.Gly435Arg
NM_016356.4:c.1303G>C NP_057440.2:p.Gly435Arg
NM_016356.5:c.1303G>C MANE Select NP_057440.2:p.Gly435Arg
NM_001195610.2:c.1303G>C NP_001182539.1:p.Gly435Arg
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